Basic information Safety Supplier Related

N-BUTYL-2-CHLORO-ACETAMIDE

Basic information Safety Supplier Related

N-BUTYL-2-CHLORO-ACETAMIDE Basic information

Product Name:
N-BUTYL-2-CHLORO-ACETAMIDE
Synonyms:
  • ASINEX-REAG BAS 02927056
  • N-BUTYL-2-CHLORO-ACETAMIDE
  • TIMTEC-BB SBB010319
  • N-BUTYL-2-CHLORACETAMIDE
  • N-butyl-2-chloro-ethanamide
  • Acetamide, N-butyl-2-chloro-
CAS:
5349-24-6
MF:
C6H12ClNO
MW:
149.62
Mol File:
5349-24-6.mol
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N-BUTYL-2-CHLORO-ACETAMIDE Chemical Properties

Melting point:
96.5 °C(Solv: benzene (71-43-2))
Boiling point:
110 °C(Press: 7.0 Torr)
Density 
1.032±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
14.38±0.46(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22
HazardClass 
IRRITANT
HS Code 
2924297099
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N-BUTYL-2-CHLORO-ACETAMIDE Usage And Synthesis

Synthesis

109-73-9

79-04-9

5349-24-6

GENERAL STEPS: Chloroacetyl chloride (0.2 mol, 15.9 mL, CAS: 79-04-9) was slowly added dropwise to a solution of dichloromethane (50 mL) containing n-butylamine (0.2 mol, 14.83 g) in an ice bath. After the dropwise addition, 20% NaOH aqueous solution was added and the reaction mixture was warmed up to room temperature and stirring was continued for 2 hours. After completion of the reaction, the organic phase was separated and washed sequentially with 5% aqueous HCl and 5% aqueous NaHCO3 (3 x 25 mL each). The organic phase was dried and filtered, and then the solvent was removed by distillation under reduced pressure to give the intermediate N-butyl-2-chloroacetamide (92% yield). Subsequently, the intermediate (0.05 mol, 9.00 g) was mixed with 5,6,7,8-tetrahydropyrido[1,2-α]imidazole (0.05 mol, 6.11 g, CAS: 34167-66-3) in acetonitrile (50 mL) and the reaction was carried out at reflux for 18 hours. The reaction solution was recrystallized by ethyl acetate recrystallization operation to give the product [4C-imCH2CONHBu]Cl (89% yield). Finally, [4C-imCH2CONHBu]OH was obtained by treatment with anion exchange resin.

References

[1] Patent: CN104326949, 2016, B. Location in patent: Paragraph 0060; 0061; 0063
[2] Patent: WO2007/9083, 2007, A2. Location in patent: Page/Page column 68
[3] ACS Medicinal Chemistry Letters, 2017, vol. 8, # 6, p. 678 - 681
[4] ChemMedChem, 2018,
[5] Organic Letters, 2004, vol. 6, # 26, p. 4805 - 4808

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